Duloxetine

NDC 47335-381 · Sun Pharmaceutical Industries, Inc.

Generic nameDuloxetine

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)DULOXETINE HYDROCHLORIDE

Strength20 mg/1

Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Marketing categoryANDA

Packages

47335-381-08 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-08)

47335-381-18 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-18)

47335-381-61 — 100 BLISTER PACK in 1 CARTON (47335-381-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

47335-381-83 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-83)

47335-381-86 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-86)

47335-381-88 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-381-88)

FDA lists these products with the same active ingredient.

33342-160 — Duloxetine Hydrochloride, 33342-161 — Duloxetine Hydrochloride, 33342-162 — Duloxetine Hydrochloride, 42708-196 — Duloxetine, 43547-379 — Duloxetine, 43547-380 — Duloxetine, 43547-381 — Duloxetine, 46708-278 — Duloxetine, 46708-279 — Duloxetine, 46708-280 — Duloxetine, 47335-382 — Duloxetine, 47335-383 — Duloxetine, 47335-616 — Duloxetine, 47335-617 — Duloxetine, 47335-618 — Duloxetine, 47335-619 — Duloxetine, 49252-007 — duloxetine, 49252-008 — duloxetine, 49252-009 — duloxetine, 50090-3205 — DULOXETINE HYDROCHLORIDE, +188 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.